Intracellular location and nuclear targeting of the Spi-1, Spi-2 and Spi-3 gene-derived serine protease inhibitors in non-secretory cells
| Autor: | Tore Kempf, Hermann Stammer, Tova Glaser, Dieter Werner, Benediktas Juodka, Karsten Rothbarth |
|---|---|
| Rok vydání: | 2001 |
| Předmět: |
Signal peptide
Proteases Serine Proteinase Inhibitors animal structures Histology medicine.medical_treatment Green Fluorescent Proteins Molecular Sequence Data Nuclear Localization Signals Gene Expression Biology Transfection Pathology and Forensic Medicine Viral Proteins Tumor Cells Cultured medicine Animals Amino Acid Sequence Carcinoma Ehrlich Tumor Serpins Cell Nucleus Mammals Serine protease Protease Cell Cycle DNA Cell Biology General Medicine Proteinase K Fusion protein Chromatin Cell biology Luminescent Proteins Microscopy Fluorescence Biochemistry biology.protein Intercellular Signaling Peptides and Proteins Indicators and Reagents Peptides Intracellular Acute-Phase Proteins |
| Zdroj: | European Journal of Cell Biology. 80:341-348 |
| ISSN: | 0171-9335 |
| DOI: | 10.1078/0171-9335-00170 |
| Popis: | Summary Proteases and their inhibitors are indispensable for the regulated activation and/or degradation of structural and functional proteins involved in basic cellular processes, e.g. in cell cycle control, cell growth, differentiation and apoptosis. In this context the serine protease inhibitors derived from the murine Spi-1, Spi-2 and Spi-3 genes, and their human homologs, deserve reconsideration. Microsequencing data indicate that a fraction of the three serpins has the capability to constitute a well characterized proteinase K, high salt and SDS-stable complex which coisolates with DNA under salting out conditions from various cell and tissue types. This tight association with DNA isolated under conditions designed to deproteinize DNA efficiently points to an in situ preformed chromatin complex. Accordingly, in addition to their well known functions as ‘serum protease inhibitors’ the Spi-1 and Spi-2 gene-derived proteins appear to have intracellular functions as well. The involvement of the three serpins in chromatin complexes requires their nuclear translocation. Application of (enhanced) green fluorescent protein technology and optical section microscopy reveals that truncation of the N-terminal signal sequences of the Spi-1 and Spi-2 gene-encoded proteins is a prerequisite for their nuclear translocation while non-truncated fusion proteins are enriched at the nuclear indentation which is the site of the Golgi apparatus and the centrosome. The identification of new species of intracellular serpins is of potential interest with respect to accumulating evidence for serine protease inhibitor-dependent inhibition or prevention of apoptosis. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full Text from ScienceDirect